Hishinuma A - Search Results

1

Genetic alteration of ARMC5 in a patient diagnosed with meningioma and primary macronodular adrenal hyperplasia: a case report.

Jojima T, Kogai T, Iijima T, Kato K, Sagara M, Kezuka A, Kase M, Sakurai S, Akimoto K, Sakumoto J, Namatame T, Ueki K, Hishinuma A, Kamai T, Usui I, Aso Y. Jojima T, et al. Among authors: hishinuma a. Eur J Endocrinol. 2020 Dec;183(6):K7-K12. doi: 10.1530/EJE-20-0014. Eur J Endocrinol. 2020. PMID: 33105102

2

A novel missense mutation (G2320R) in thyroglobulin causes hypothyroidism in rdw rats.

Hishinuma A, Furudate S, Oh-Ishi M, Nagakubo N, Namatame T, Ieiri T. Hishinuma A, et al. Endocrinology. 2000 Nov;141(11):4050-5. doi: 10.1210/endo.141.11.7794. Endocrinology. 2000. PMID: 11089535

3

Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis.

Hishinuma A, Ohyama Y, Kuribayashi T, Nagakubo N, Namatame T, Shibayama K, Arisaka O, Matsuura N, Ieiri T. Hishinuma A, et al. Eur J Endocrinol. 2001 Oct;145(4):385-9. doi: 10.1530/eje.0.1450385. Eur J Endocrinol. 2001. PMID: 11580993

4

TTF-2 stimulates expression of 17 genes, including one novel thyroid-specific gene which might be involved in thyroid development.

Hishinuma A, Ohmika N, Namatame T, Ieiri T. Hishinuma A, et al. Mol Cell Endocrinol. 2004 Jun 30;221(1-2):33-46. doi: 10.1016/j.mce.2004.04.003. Mol Cell Endocrinol. 2004. PMID: 15223130

5

Familial hypocalciuric hypercalcemia with a de novo heterozygous mutation of calcium-sensing receptor.

Taki K, Kogai T, Sakumoto J, Namatame T, Hishinuma A. Taki K, et al. Among authors: hishinuma a. Endocrinol Diabetes Metab Case Rep. 2015;2015:150016. doi: 10.1530/EDM-15-0016. Epub 2015 May 1. Endocrinol Diabetes Metab Case Rep. 2015. PMID: 26019872 Free PMC article.

6

Graves' disease and Gitelman syndrome.

Mizokami T, Hishinuma A, Kogai T, Hamada K, Maruta T, Higashi K, Tajiri J. Mizokami T, et al. Among authors: hishinuma a. Clin Endocrinol (Oxf). 2016 Jan;84(1):149-50. doi: 10.1111/cen.12829. Epub 2015 Jul 3. Clin Endocrinol (Oxf). 2016. PMID: 26041598 No abstract available.

7

Iodide Transport Defect and Breast Milk Iodine.

Mizokami T, Fukata S, Hishinuma A, Kogai T, Hamada K, Maruta T, Higashi K, Tajiri J. Mizokami T, et al. Among authors: hishinuma a. Eur Thyroid J. 2016 Jul;5(2):145-8. doi: 10.1159/000446496. Epub 2016 May 27. Eur Thyroid J. 2016. PMID: 27493890 Free PMC article.

8

A Novel Germline Mutation of KEAP1 (R483H) Associated with a Non-Toxic Multinodular Goiter.

Nishihara E, Hishinuma A, Kogai T, Takada N, Hirokawa M, Fukata S, Ito M, Yabuta T, Nishikawa M, Nakamura H, Amino N, Miyauchi A. Nishihara E, et al. Among authors: hishinuma a. Front Endocrinol (Lausanne). 2016 Sep 20;7:131. doi: 10.3389/fendo.2016.00131. eCollection 2016. Front Endocrinol (Lausanne). 2016. PMID: 27703446 Free PMC article.

9

PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule.

Nyuzuki H, Kogai T, Hishinuma A, Ogawa Y, Saitoh A, Nagasaki K. Nyuzuki H, et al. Among authors: hishinuma a. Pediatr Int. 2017 Nov;59(11):1223-1224. doi: 10.1111/ped.13427. Pediatr Int. 2017. PMID: 29359449 No abstract available.

10

Congenital Primary Hypothyroidism with the Homozygous Nonsense Mutation P.K1374* in the Thyroglobulin Gene and a Normal-sized Thyroid Gland on Levothyroxine Replacement.

Mizokami T, Fukata S, Kogai T, Hishinuma A, Hamada K, Maruta T, Higashi K, Tajiri J. Mizokami T, et al. Among authors: hishinuma a. Intern Med. 2019 Sep 15;58(18):2669-2673. doi: 10.2169/internalmedicine.1163-18. Epub 2019 Jun 7. Intern Med. 2019. PMID: 31178475 Free PMC article.

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